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Asymmetric catalysis heterogeneous

The coordination of ligands at the surface of metal nanoparticles has to influence the reactivity of these particles. However, only a few examples of asymmetric heterogeneous catalysis have been reported, the most popular ones using a platinum cinchonidine system [65,66]. In order to demonstrate the directing effect of asymmetric ligands, we have studied their coordination on ruthenium, palladium, and platinum nanoparticles and the influence of their presence on selected catalytic transformations. [Pg.248]

Asymmetric Heterogeneous Catalysis Using Supported Metal Complexes... [Pg.44]

The transformations that use asymmetric heterogeneous catalysis will be highlighted P-keto esters and diketone reductions by Raney nickel catalyst modified with R,R-tartaric acid and NaBr. a-Keto acid reductions with cinchona modified Pt catalysts are discussed in Chapter 18. [Pg.229]

Heitbaum M, Glorius E, Escher I. Asymmetric heterogeneous catalysis. Angew. Chem., Int. Ed. 2006 45 4732-4762. [Pg.2137]

M. Nielsen, A. H. Thomsen, T. R. Jensen, H. J. Jakobsen, J. Skibsted, K. V. Gothelf, Pormation and structure of conjugated salen-cross-linked polymers and their application in asymmetric heterogeneous catalysis, Eur. ]. Org. Ghem. (2005) 342. [Pg.408]

Handbook of Asymmetric Heterogeneous Catalysis. Edited by K. Ding and Y. Uozumi Copyright 2008 WILEY-VCH Verlag GmbH Co. KGaA, Weinheim ISBN 978-3-527-31913-8... [Pg.1]

It is the goal of this chapter to present an overview of asymmetric heterogeneous catalysis using inorganic supports, thereby portraying the state of the art and discussing its potential and limitations. [Pg.27]

If an asymmetric catalyst acts perfectly well from the point of view of enanti-oselectivity and activity, there remains one difficulty to overcome, namely the recovery and the reuse of the catalyst. This can be achieved by asymmetric heterogeneous catalysis. This old approach, where a metal was modified by a chiral additive [12,14], has been reappraised recently, giving interesting results, but the scope of the reaction remains very narrow (see the review in Ref. [ 122]). [Pg.40]

A Baiker. Progress in asymmetric heterogeneous catalysis Design of novel chirally modified platinum metal catalysts. J Mol Catal A Chem 115 473-493,1997. [Pg.365]

The synthetic method described above is very simple and can be in principle transposed to any metal/ligand combination. One of the most challenging problems regarding the use of nanoparticles in catalysis concerns asymmetric catalysis. Only a few examples of asymmetric heterogeneous catalysis have been reported, the most popular ones based on a platinum cinchonidine system. Using the chiral xylofuranoside diphosphite ligand, Pd nanoparticles with a... [Pg.80]

Asymmetric heterogeneous catalysis has been demonstrated by the enantioselec-tive and racemic hydrogenation of ethyl pyruvate over Pt-Al203 catalyst. Higher reaction rate and enantioselectivity (75%) were observed in nonpolar solvent (toluene) whereas in a polar solvent (ethanol) they decreased substantially (Scheme 13.5) [58]. [Pg.624]

Herault,D., Saluzzo,C., Duval,R., Lamaire,M. (2002) Enantiopine beds a tool for asymmetric heterogeneous catalysis, J. Mol. Catal. A. Chem. 182-183, 249-256. [Pg.241]


See other pages where Asymmetric catalysis heterogeneous is mentioned: [Pg.370]    [Pg.396]    [Pg.401]    [Pg.340]    [Pg.460]    [Pg.823]    [Pg.346]    [Pg.247]    [Pg.18]    [Pg.359]    [Pg.455]    [Pg.456]    [Pg.458]    [Pg.468]    [Pg.469]    [Pg.71]    [Pg.312]    [Pg.57]   
See also in sourсe #XX -- [ Pg.111 , Pg.112 , Pg.113 , Pg.140 , Pg.141 ]




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Handbook of Asymmetric Heterogeneous Catalysis. Edited by K. Ding and Y. Uozumi

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